17 results on '"Evin, Ferda"'
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2. Predictive low-glucose suspend system and glycemic variability
3. Effectiveness of whole exome sequencing analyses in the molecular diagnosis of osteogenesis imperfecta.
4. The Relationship Between Premature Adrenarche and Markers of Inflammation in Complete Blood Count.
5. Basal and Bolus Insulin Distribution According to Treatment Modality: Data from SWEET Diabetes Registry
6. A case-control study of early-stage radiological markers of endothelial dysfunction and cardiovascular findings in patients with osteogenesis imperfecta: genotype–phenotype correlations.
7. ABCC8-related maturity-onset diabetes of the young: switching from insulin to sulphonylurea therapy: how long do we need for a good metabolic control?
8. Molecular genetic etiology by whole exome sequence analysis in cases with familial type 1 diabetes mellitus without HLA haplotype predisposition or incomplete predisposition
9. Prediction of Transient or Permanent Congenital Hypothyroidism
10. Early-Stage Radiological Markers of Endothelial Dysfunction and Cardiovascular Findings in Patients with Osteogenesis Imperfecta and Their Genotype-Phenotype Correlations: A Case-Control Study
11. Evaluation of the Frequency of Multiple Hormone Deficiency and Long-Term Data in Patients with Craniopharyngioma
12. Detection of Copy Number Variations by Microarray in Disorders of Sex Development of Unexplained Molecular Etiology and Association with Clinical Findings
13. The Value of Telemedicine for the Follow-up of Patients with New Onset Type 1 Diabetes Mellitus During COVID-19 Pandemic in Turkey: A Report of Eight Cases
14. Molecular genetic etiology by whole exome sequence analysis in cases with familial type 1 diabetes mellitus without HLA haplotype predisposition or incomplete predisposition.
15. Evaluation of Digit Ratios in Youth With Polycystic Ovary Syndrome.
16. "Predicting diabetic kidney disease in youth with type 1 diabetes: Insights from genetic risk assessment".
17. Molecular Genetic Diagnosis with Targeted Next Generation Sequencing in a Cohort of Turkish Osteogenesis Imperfecta Patients and Their Genotype-phenotype Correlation.
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